Welcome to the Coats' Disease Patient Insights Network

  

Join patients around the world in building the PIN community.

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Find out about research studies and clinical trials.

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Advance research and speed development of new treatments.

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Connecting you with researchers who can make a difference

At the Jack McGovern Coats’ Disease Foundation, our mission is to enable new insights into the study of Coats’ Disease. As we continue to work toward finding a cure, a major challenge to researchers is the lack of correctly diagnosed patients to participate in medical research.
 
That’s why we are creating the first and only Coats’ disease Patient Insights Network (PIN). Through this PIN, medical researchers will be able to tap into the pool of Coats’ disease patients for their work, furthering an understanding of the disease. By joining this network and providing your information, you help the Coats’ disease community gain knowledge and facilitate research. Your data is fully secured and de-identified, meaning no researchers will see who you are, your data, and there are no obligations to participate actively in any studies.
 
By joining the Coats’ disease PIN, together we make strides toward finding better treatments and ultimately, a cure. 

Click here to register now!

Connecting you with researchers who can make a difference

At the Jack McGovern Coats’ Disease Foundation, our mission is to enable new insights into the study of Coats’ Disease. As we continue to work toward finding a cure, a major challenge to researchers is the lack of correctly diagnosed patients to participate in medical research.
 
That’s why we are creating the first and only Coats’ disease Patient Insights Network (PIN). Through this PIN, medical researchers will be able to tap into the pool of Coats’ disease patients for their work, furthering an understanding of the disease. By joining this network and providing your information, you help the Coats’ disease community gain knowledge and facilitate research. Your data is fully secured and de-identified, meaning no researchers will see who you are, your data, and there are no obligations to participate actively in any studies.
 
By joining the Coats’ disease PIN, together we make strides toward finding better treatments and ultimately, a cure. 

LEARN MORE